Variant report

Variant rs6909041
Chromosome Location chr6:167622697-167622698
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167614400-167623200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr6:167615800-167628800 Weak transcription Right Atrium heart
3 chr6:167618400-167624400 Weak transcription Colon Smooth Muscle Colon
4 chr6:167619000-167624200 Weak transcription Rectal Smooth Muscle rectum
5 chr6:167621000-167623600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr6:167621200-167623000 Weak transcription Fetal Brain Male brain
7 chr6:167621600-167624400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr6:167622200-167623000 Enhancers H1 Cell Line embryonic stem cell
9 chr6:167622200-167623000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr6:167622200-167624600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:167622200-167624600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr6:167622400-167622800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr6:167622400-167622800 Enhancers Fetal Intestine Large intestine
14 chr6:167622400-167623200 Enhancers Fetal Intestine Small intestine
15 chr6:167622400-167626600 Enhancers Placenta Amnion Placenta Amnion
16 chr6:167622400-167627200 Enhancers HepG2 liver
17 chr6:167622600-167623000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell

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